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Ferrochelatase pseudogene 1 (FECHP1) is a processed pseudogene located at human chromosome 3p22-p23, closely related in nucleotide sequence (>80% identity) to the functional ferrochelatase gene (FECH) but lacking intronic regions and containing multiple genetic disruptions that prevent protein expression. It does not encode a functional polypeptide, is not transcribed in detectable amounts in erythroid cells, and is not involved in heme biosynthesis. Its main significance is in genetic studies related to ferrochelatase deficiency and heme biosynthesis disorders, where it may complicate gene mapping or mutation detection efforts. No direct disease roles, biological functions, or drug interactions are established.
None; no drugs target this pseudogene.
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